Your search for "bcr" returned 4,472 TaqMan® SNP Genotyping Assays
BCR, RhoGEF and GTPase activating protein
A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this translocation is located within the BCR gene. The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL, the gene at the chromosome 9 breakpoint. Although the BCR-ABL fusion protein has been extensively studied, the function of the normal BCR gene product is not clear. The protein has serine/threonine kinase activity and is a GTPase-activating protein for p21rac. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
5133400C09RIK, AI561783, AI853148, ALL, BCR, BCR1, CML, D22S11, D22S662, MKIAA3017, PHL
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